반응 #83128

반응 방정식

2-adamantyloxycarbonyl-α-methyl-DL-tryptophan

1-hydroxybenzotriazole hydrate

1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

3-[2-aminoethyl)benzo[b]thiophene hydrochloride

Et3N

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product

Tricyclo[3.3.1.13,7 ]dec-2-yl (±)-[2-[[2-(benzo[b]thien-3-yl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamate

용매

DMF

반응 조건

후처리

1. 1
   workup.STIRRINGstirred for an additional 18 hours
2. 2
   기타The reaction mixture was partitioned between 100 mL of EtOAc and 150 mL of H2O
3. 3
   기타The layers were separated
4. 4
   추출the aqueous layer extracted with fresh EtOAc (3×75 mL)
5. 5
   세척The combined organic layers were washed with 5% aqueous citric acid (3×150 mL), brine (1×150 mL), 5% aqueous NaHCO3 (3×150 mL), and brine again
6. 6
   건조The organic layer was dried (Na2SO4)
7. 7
   기타evaporated (vacuum) to an off-white foam
8. 8
   기타The residue was chromatographed (230-400 mesh SiO2 in a 21×300 mm column
9. 9
   세척eluted with 2% MeOH in CH2Cl2)

실험 절차

A solution of 0.50 g (1.26 mmol) of 2-adamantyloxycarbonyl-α-methyl-DL-tryptophan and 0.18 g (1.33 mmol) of 1-hydroxybenzotriazole hydrate in 8 mL of anhydrous DMF (under a N2 atmosphere) was treated in one portion with 0.27 9 (1.41 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride. The mixture was stirred at room temperature for 2 hours, treated with 0.30 g (1.40 mmole) of 3-[2-aminoethyl)benzo[b]thiophene hydrochloride plus 0.25 mL (0.18 g, 1.79 mmol) of Et3N, and stirred for an additional 18 hours. The reaction mixture was partitioned between 100 mL of EtOAc and 150 mL of H2O. The layers were separated and the aqueous layer extracted with fresh EtOAc (3×75 mL). The combined organic layers were washed with 5% aqueous citric acid (3×150 mL), brine (1×150 mL), 5% aqueous NaHCO3 (3×150 mL), and brine again. The organic layer was dried (Na2SO4) and evaporated (vacuum) to an off-white foam. The residue was chromatographed (230-400 mesh SiO2 in a 21×300 mm column, eluted with 2% MeOH in CH2Cl2) to yield the purified product as a white foam, 0.40 g (57%); 1H NMR (CDCl3) δ1.47-1.92 (17H, m), 2.92 (2H, t, J 7 Hz), 3.25 (1H, d, J 15 Hz), 3.46-3.57 (3H, m), 4.79 (1H, br s), 5.14 (1H, br s), 6.27 (1H, m), 7.02 (2H, m), 7.11-7.86 (8H, m), 8.10 (1H, br s).

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